Cocaine receptor binding ligands

ABSTRACT

The invention relates to novel compounds which show high affinity for cocaine receptors in the brain, particularly dopamine and serotonin transporter sites. The compounds may be used as imaging or pharmaceutical agents, in the diagnosis and treatment of drug addiction, depression, anorexia and neurodegenerative diseases.

[0001] This application is a continuation-in-part application of U.S. patent application Ser. No. 08/706,263, filed Sep., 4, 1996, which is a continuation in part of U.S. patent application Ser. No. 08/506,541, filed Jul. 24, 1995, which is a continuation-in-part of (1) U.S. patent application Ser. no. 07/972,472, filed Mar. 23, 1993, which issued May 9, 1995 as U.S. Pat. No. 5,413,779; (2) U.S. patent application Ser. No. 08/164,576, filed Dec. 10, 1993, which is in turn a continuation-in-part of U.S. patent application Ser. No. 07/792,648, filed Nov. 15, 1991, now U.S. Pat. No. 5,380,848, which is in turn a continuation-in-part of U.S. patent application Ser. No. 07/564,755, filed Aug. 9, 1990, now U.S. Pat. No. 5,128,118 and U.S. PCT Application PCT/US91/05553, filed Aug. 9, 1991, filed in the U.S. PCT Receiving Office and designating the United States; and (3) U.S. patent application Ser. No. 08/436,970, filed May 8, 1995, all of which are incorporated herein by reference in their entirety.

FIELD OF THE INVENTION

[0002] This invention is directed to a class of binding ligands for cocaine receptors and other receptors in the brain. Specifically, a novel family of compounds shows high binding specificity and activity, and, in a radiolabeled form, can be used to bind to these receptors, for biochemical assays and imaging techniques. Such imaging is useful for determining effective doses of new drug candidates in human populations. In addition, the high specificity, slow onset and long duration of the action of these compounds at the receptors makes them particularly well suited for therapeutic uses, for example as substitute medication for psychostimulant abuse. Some of these compounds may be useful in treating Parkinson's Disease or depression, by virtue of their inhibitory properties at monoamine transporters.

DISCLOSURE OF PARENT APPLICATIONS

[0003] This application claims priority, inter alia, from of U.S. patent application Ser. No. 07/972,472 filed Mar. 23, 1993, now U.S. Pat. No. 5,413,779, the entirety of which is incorporated by reference. This application also claims priority from U.S. patent application Ser. No. 07/564,755, now U.S. Pat. No. 5,128,118, and U.S. PCT Application PCT/US91/05553 (the U.S. National Phase of which is U.S. Ser. No. 07/972,472), filed Aug. 9, 1991, both applications being incorporated herein by reference. In U.S. application Ser. No. 07/564,755, there is disclosure of a family of compounds exhibiting particularly high specificity and affinity for cocaine receptors and other neurotransmitter receptors in the brain of the formula:

[0004] Where the broken line represents an optional chemical bond and the substituents at 2 and 3 may be at any position;

[0005] The iodo substituent may be at o, m, A, or multisubstituted;

[0006] R₁=CH₃, CH₂CH═CH₂, (CH₂)_(n)C₆H₅ n=1-4;

[0007] R₂=CH₃, C₂H₅, CH₃(CH₂)₃, (CH₃)₂CH, C₆H₅, C₆H₅CH₂, C₆H₅(CH₂)₂;

[0008] X=pharmacologically acceptable anion

[0009] Sites of specific interest included cocaine receptors associated with dopamine (DA) transporter sites.

[0010] Subsequently, in the U.S. PCT Application from which priority is claimed, and which is incorporated herein by reference, the values for R₁ and R₂ were expanded, such that R may be an alkyl of 1-7 carbon atoms, CH₂CR₃═CR₄R₅ wherein R₃-R₅ are each, independently C₁₋₆ alkyl, or phenyl compounds of the formula C₆H₅(CH₂)_(y), wherein y=1-6. R₂ may be any of those list above and also C₆H₅(CH₂)_(z), wherein z=1-6. The PCT filing also reveals the affinity of these compounds for cocaine receptors associated with serotonin (5-hydroxytryptamine, 5-HT) transporters, and confirms, for the first time, that the in vitro binding reported in the earlier-filed application, is confirmed in in vivo testing. Specific disclosure for a variety of applications, including using the compounds in both PET and SPECT scanning, wherein either the iodine substituent, or one of the carbon groups is radioactive (I-123, 125 or 131 and C₁₁) thus providing methods for scanning for the presence of specific cocaine receptors. Such scanning processes may be used to determine physiological conditions associated with dopamine and serotonin re-uptake inhibitors, which lead to behavioral and neurodegenerative disorders/diseases. Such disorders include depression, bipolar disorder, eating disorders, obesity, attention deficit disorder, panic attacks and disorders, obsessive-compulsive disorder, Parkinson's Disease, and cocaine, nicotine and alcohol addiction. These compounds, in addition to being used in treatment of these disorders, may be used to examine in general the density and distribution of specific cocaine receptors in various parts of the brain and/or body, to determine the efficacy of neurological treatments aimed at halting or reversing the degeneration of specific nerves in the brain, and for screening drugs, such as antidepressant drugs.

[0011] The affinity and specificity of these compounds, as reported in the applications incorporated, is surprisingly high, and compared with prior art compounds, such as [³H]WIN 35,428, the novel compounds of these applications exhibit extremely low IC₅₀ values for binding inhibition.

[0012] In U.S. patent application Ser. No. 08/164,576, filed Dec. 10, 1993, now U.S. Pat. No. 5,496,953, also incorporated herein by reference in its entirety, a family of compounds was disclosed, having the formula:

[0013] wherein

[0014] Y is CONRR₂,

[0015] R₁ is hydrogen or C₁₋₅ alkyl,

[0016] X is H, C₁₋₆ alkyl, C₃₋₈, cycloalkyl, C₁₋₄, alkoxy, C₁₋₆ alkynl, halogen amino or acylamido,

[0017] R and R₂ independently are H, C₁₋₆ alkyl, alkene or alkyne, phenyl, phenyl substituted with 1-3 Of C₁₋₆ alkyl, alkene, alkyne or alkoxy, C₁₋₆ alkoxy, phenoxy, amine amino substituted with 1 or 2 C₁₋₆ alkyl, alkene, alkyne, alkoxy, phenyl or phenoxy, or R and R₂ may combine to form a cyclic structure selected from the group consisting of pyrrolidinyl, morpholinyl and piperidinyl moieties, and

[0018] Z is H, I, Br, Cl, F, CN, CF₃, NO₂, N₃, OR₁, CO₂NH₂, CO₂R₁, C₁₋₆ alkyl, NR₄R₅, NHCOF₅, NHCOR₆, wherein R₄-R₆ are each C₁₋₆ alkyl.

[0019] These compounds exhibit unusually high affinity and specificity for binding to receptors for the dopamine transporter site, as well as the serotonin transporter site, based on inhibition of [³H]paroxetine binding. This high affinity makes certain of these compounds particularly well suited for use as therapeutic agents, as well as for imaging agents for dopamine and serotonin transporters.

SUMMARY OF THE INVENTION

[0020] Accordingly, one object of this invention is to provide novel compounds which bind to cocaine receptors.

[0021] Another object of the invention is to provide novel 3-(substituted phenyl)-2-(substituted)tropane analogs which bind to cocaine receptors.

[0022] Still another object of the invention is to provide 3-(substituted phenyl)-2-(substituted)tropane analogs which bind preferentially to the dopamine transporter.

[0023] Yet another object of the invention is to provide 3-(substituted phenyl)-2-(substituted)tropane analogs which bind preferentially to the serotonin transporter.

[0024] Another object of the invention is to provide a compound of the formula

[0025] wherein R is CH₃, C₂H₅, CH₂CH₂CH₃, or CH(CH₃)₂, R₁ is CH₃, CH₂CH₅, (CH₂)₂C₆H₅, (CH₂)₃C₆H₅, or

[0026] wherein X is H, OCH₃, or Cl and Y is H, OCH₃, CO₂CH₃ or Cl, and n=1l-8.

[0027] Another object of the invention is to provide compounds having the following formulas:

[0028] wherein

[0029] R₁=hydrogen, C₁₋₅ alkyl,

[0030] X=H, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₆ alkynyl, halogen, amino, acylamido, and

[0031] Z=H, I, Br, Cl, F, CN, CF₃, NO₂, N₃, OR₁, CONH₂, CO₂R₁, C₁₋₆ alkyl, NR₄R₅, NHCOR₅, NHCO₂R₆,

[0032] R_(b) is C₁₋₆ alkyl, C₁₋₆ alkenyl, phenyl, or phenyl substituted with C₁₋₆ alkyl, C₁₋₆ alkoxy, or halogen;

[0033] wherein R₁=H or CO₂CH₃;

[0034] wherein R₁, R₂=H or CH₃ and X=CH₃;

[0035] wherein R=H, CH₃ or CH₂CO₂C₂H₅,

[0036] and Y=H , X=CH₃, Cl, t-CH₃CH═CH—, 2-naphthyl, or H₂C═C—;

[0037] wherein R=CH₃, C₆H₅, 4-CH₃OC₆H₄, 4-ClC₆H₄, 4-BrC₆H₄, or (CH₃)₂CH and X=Cl, CH₃ or H; and

[0038] wherein X=CH₃ or H and Y=H or CH₃.

[0039] A further object of the invention is to provide a method for treating psychostimulant abuse, by administering to a patient in need of such treatment a pharmaceutically effective amount of a 3-(substituted phenyl)-2-(substituted)tropane analog.

[0040] A still further object of the invention is to provide method for inhibiting the action of a psychostimulant, by administering to a patient in need of such treatment a psychostimulant-inhibiting amount of a 3-(substituted phenyl)-2-(substituted)tropane analog.

[0041] Still another object of the invention is to provide a method for inhibiting neurotransmitter re-uptake by administering to a patient in need of such treatment a neurotransmitter transporter-inhibiting amount of a 3-(substituted phenyl)-2-(substituted)tropane analog.

[0042] Another object of the invention is to provide a method for treating neurodegenerative disorders, by administering to a patient in need of such treatment a pharmaceutically effective amount of a 3-(substituted phenyl)-2-(substituted)tropane analog.

[0043] Still another object of the invention is to provide a method for treating depression, by administering to a patient in need of such treatment a pharmaceutically effective amount of a 3-(substituted phenyl)-2-(substituted)tropane analog.

[0044] Briefly, the invention pertains to the discovery that certain cocaine analogs are particularly well suited for therapeutic use as neurochemical agents. These particular cocaine analogs, in modulating neurotransmitter actions, may also be useful for modulating the actions of pyschostimulant drugs, for modulating endocrine function, for modulating motor function, and for modulating complex behaviors.

[0045] With the foregoing and other objects, advantages and features of the invention that will become here in after apparent, the nature of the invention may be more clearly understood by reference to the following detailed description of the preferred embodiments of the invention and to the appended claims.

BRIEF DESCRIPTION OF THE DRAWINGS

[0046] A more complete appreciation of the invention and many of the attendant advantages thereof will be readily obtained as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings, wherein:

[0047]FIG. 1 depicts the scheme for converting 3-(substituted phenyl)-2-tropane carboxylic acid (tropane acid) to 2-substituted tetrazoles, oxazoles, oxadiazoles, thiazoles, thiadiazoles and benzothiazole.

[0048]FIG. 2 depicts the scheme in which the carboxamide obtained from the tropane acid was treated to obtain nitrites and tetrazoles.

[0049]FIG. 3 depicts the scheme used to prepare 3-substituted isoxazoles.

[0050]FIG. 4 depicts the scheme for converting RTI-93 to RTI-123.

[0051]FIG. 5 depicts the scheme for converting a 3β-phenyltropane 2β-ester analog(RTI-32) to a 3β-phenyltropane 2β-amide analog (RTI-129) and a 3β-phenyltropane 2β-aminomethyl analog (RTI-132).

[0052]FIG. 6 depicts the scheme for converting a 3β-phenyltropane analog (RTI-31)or a 3β-phenyltropane 2ρ-ester analog(RTI-32) into a 3β-phenyltropane 2β-(3′-substituted-1,2,4-oxadiazol-5-yl) analog (RTI-144) or a 3β-phenyltropane 2p-heterocyclic analog (RTI-194, RTI-219, and RTI-202).

[0053]FIG. 7 depicts the scheme for converting a 3p-phenyltropane analog (RTI-31) into a 3β-phenyltropane 2β-amide analog (RTI-214).

[0054]FIG. 8 depicts the scheme for making a 3p-phenyltropane 2P-alkyl analog (RTI-239).

[0055]FIG. 9 depicts the scheme for making a 3P-phenyltropane analog (RTI-251) and an N,C2-fused 3β-phenyltropane analog (RTI-242).

[0056]FIG. 10 depicts the scheme for making RTI compounds 296, 298 and 309.

[0057]FIG. 11 depicts the scheme for making RTI-318.

[0058]FIG. 12 depicts the scheme for making a 2β,3β-diphenyltropane analog (RTI-422).

DETAILED DESCRIPTION OF THE INVENTION

[0059] The present invention includes novel compounds having the following formula:

1a, R = C₂H₅b, R = CH₂CH₃CH₃c, R = CH(CH₃)₃

2a, R₁ = CH₂C₆H₅b, R₁ = (CH₂)₂C₆H₅c, R₁ = (CH₂)₃C₆H₅

3a, X = H, Y = OCH₃b, X = OCH₃, Y = H c, X = OCH₃, Y = OCH₃d, X = Cl, Y = H e, X = H, Y = Cl f, X = Cl, Y = Cl

1a, R₁ = H 1b, R₁ = CO₂CH₃

1a, Y = CO₂CH₃M = C≡C R₁ = CH₃X = H Z = H

1a, X = CH₃Y = H 1b, X = H Y = H 1c, X = H Y = CH₃

1a, R₁, R₂, X = CH₃1b, R₁, X = CH₃R₂ = H 1c, R₁, R₂ = H X = CH₃

1a, R = C₆H₄X = Cl 1b, R = 4-CH₃OC₆H₄X = Cl 1c, R = C₆H₅X = CH₃

1a, R = CH₃, X = t-CH₃CH═CH 1b, R = CH₃, X = CH₃C≡C 1c, R = CH₃, X = 2-naphthyl 1d, R = H, X = H_(C≡C)1e, R = CH₂CO₂C₂H₅X = Cl

X = Cl 1b, R = CON(CH₃)₂X = Cl 1c, R = CH(CH₃)₂X = CH₃1d, R =

X = Cl 1e, R =

X = Cl 1f, R =

X = CH₃1g, R = CH₂OCOC₆H₅X = Cl

[0060] The compounds of this invention can be prepared according to the synthesis methods described in the parent applications. Alternative synthesis for related compounds will be apparent to those of ordinary skill in the art. Particular synthesis schemes are exemplified in U.S. Pat. No. 5,444,070, which is incorporated herein in its entirety. Additional schemes follow hereinbelow.

[0061] Preparation of 3β-(Substituted phenyl)tropane-2β-heterocyclic Analogues

[0062] Chemistry

[0063] The known 3β-(substituted phenyl)-2β-tropane carboxylic acid (tropane acid) (Carroll et al., J. Med. Chem. 35:1813-1817 (1992)) served as the starting material for the synthesis of 2-substituted tetrazoles, oxazoles, oxadiazoles, thiazoles, thiadiazoles and benzothiazole as shown in FIG. 1.

[0064] The tropane acid was refluxed with N-acetyl and benzoic hydrazide in phosphorous oxychloride to obtain the corresponding 5-substituted 1,3,4-oxadiazoles (Afanasiadi et al., Chem. Heterocyclic Compd. 397-400 (1995)). N-benzoyl hydrazide amide obtained by the reaction of the acid chloride of tropane acid with N-benzoic hydrazide was cyclized with Lawesson's reagent (El-Barbary et al., Acta Chimica Scandinavica 597-601 (1980)) in refluxing THF to the 5-substituted 1,3,4-thiadiazoles. The N-phenylacyl carboxamide obtained from tropane acid and 2-aminoacetophenone was cyclized by refluxing the amide in phosphorous oxychloride to obtain the required 5-substituted oxazoles (Carroll et al., Med. Chem. Res. 3:468 (1993)). Cyclization of the same amide with Lawesson's reagent (El-Barbary et al., 1980) in refluxing THF gave the 5-substituted thiazoles respectively. The benzothiazole was obtained without the cyclization step by the reaction of acid chloride obtained from the appropriate tropane acid with 2-aminothiophenol.

[0065] The previously reported carboxamide (Carroll et al., 1993) obtained from the tropane acid was dehydrated with trifluoroacetic acid and pyridine in THF to the nitrites (Campagna et al., Tet. Letts. 22:1813-1816 (1977)) as shown in FIG. 2. Cycloaddition of trimethylsilylazide to the nitrile afforded the corresponding tetrazoles (Saunders et al., Med. Chem. 33:1128-1138 (1990)).

[0066]FIG. 3 outlines the route used to prepare 3-substituted isoxazole. The known tropane compounds (Carroll et al., J. Med. Chem. 34:2719-2725 (1991)) were treated with dilithiated methyl or phenyl acetoneoximes, obtained by the treatment of acetone oxime, or acetophenoneoxime with n-BuLi at 0° C. The corresponding addition product was cyclized without isolation using sulfuric acid at reflux temperature to furnish the required isoxazoles (Saunders et al., 1990).

[0067] The therapeutic effects of the present cocaine analogs can be analyzed in various ways, many of which are well known to those of skill in the art. In particular, both in vitro and in vivo assay systems may be used for the screening of potential drugs which act as agonists or antagonists at cocaine receptors, or drugs which are effective to modulate neurotransmitter level or activity, in particular by binding to a transporter of that neurotransmitter.

[0068] The compounds of the invention may be prepared and labeled with any detectable moiety, in particular a radioactive element, and may then be introduced into a tissue or cellular sample. After the labeled material or its binding partner(s) has had an opportunity to react with sites within the sample, the location and concentration of binding of the compound may be examined by known techniques, which may vary with the nature of the label attached.

[0069] Illustrative in vitro assays for binding are described in Boja et al Ann. NY Acad. Sci. 654:282-291 (1992), which is incorporated herein by reference in its entirety. A particularly preferred in vitro assay involves the ability of a compound in question to displace the binding of a known labeled compound at binding sites in a tissue sample, isolated membranes or synaptosomes. Alternatively, the compounds may be analyzed by their ability to inhibit reuptake of a labelled neurotransmitter in a sample, in particular, in synaptosomes.

[0070] The compound or its binding partner(s) can also be labeled with any detectable moiety, but are preferably labelled with a radioactive element. The radioactive label can be detected by any of the currently available counting procedures, including the imaging procedures detailed in the disclosures of the parent applications. The preferred isotope may be selected from ³H, ¹¹C, ¹⁴C, ³²P, ³⁵S, ³⁶Cl, ⁵¹Cr, ⁵⁷Co, ⁵⁸Co, ⁵⁹Fe, ⁹⁰Y, ¹²⁵I, ¹³¹I, and ¹⁸⁶Re.c,

[0071] As noted in the parent disclosures, the binding of the labelled compounds may be analyzed by various imaging techniques, including positron emission tomography (PET), single photon emission computed tomography (SPECT), autoradiogram, and the like. Such imaging techniques are useful for determining effective doses of new drug candidates. By performing in vivo competition studies, it is possible to use brain imaging studies to determine the oral doses of new drug candidates, which produce significant receptor occupancy in the brain. In vivo displacement studies which determine in vivo IC50's which in turn reflect doses that occupy receptors in vivo are described in Cline et al ((1992) Synapse 12:37-46). In addition to its uses in determining in vivo potency/occupancy, these same brain imaging methods can be used to determine rate of entry of compounds into the brain (Stathis et al (1995) Psychopharmacology 119:376-384) and duration of action (Volkow et al (1995) Synapse 19:206-211).

[0072] The binding of the compounds of the invention may be at any location where a receptor for a particular psychostimulant is present, and more specifically, any location where a dopamine or serotonin transporter is present. Such locations are in general any area comprising a part of the dopamine or serotonin pathway, in particular at synapses. Examples of locations known to be associated with dopamine transport include the cerebral cortex, hypothalamus, substantia nigra, nucleus accumbens, arcuate nucleus, anterior periventricular nuclei, median eminence and amygdala. Examples of locations known to be associated with serotonin include the striatum, cerebral cortex, hypothalamus, Raphe nuclei, pre-optic area and suprachiasmatic nucleus.

[0073] By “psychostimulant” is meant any compounds whose abuse is dependent upon mesolimbic and mesocortical dopaminergic pathways. In particular, psychostimulant relates to cocaine. However, the compounds of the invention may also be used to treat abuse of compounds not traditionally classified as “psychostimulants,” but which act at a dopamine or serotonin transporter. Such abused compounds include ethanol and nicotine.

[0074] For in vivo studies, the compounds of the invention may be prepared in pharmaceutical compositions, with a suitable carrier and at a strength effective for administration by various means to a patient experiencing an adverse medical condition associated with cocaine receptor binding or neurotransmitter release and reuptake, for the treatment thereof. The action of the compounds may be analyzed by the imaging methods noted above, and also by behavioral studies. In particular, the pharmaceutical effects of the compounds of the invention may be reflected in locomotor activity, including the induction of ipsilateral rotation, stereotyped sniffing and the “swim test”, in schedule-controlled operant behavior (i.e., response for food or shock termination) or drug self-administration. In general, maximal behavioral effects are seen at near complete occupancy of transporter sites. Such protocols are described in Boja et al (1992), Balster et al Drug and Alcohol Dependence 29:145-151 (1991), Cline et al Pharm. Exp. Ther. 260:1174-1179 (1992), and Cline et al Behavioral Pharmacology 3:113-116 (1992), which are hereby incorporated herein by reference in their entireties.

[0075] A variety of administration techniques may be utilized, among them oral or parenteral techniques such as subcutaneous, intravenous, intraperitoneal, intracerebral and intracerebroventricular injections, catheterizations and the like. Average quantities of the compounds may vary in accordance with the binding properties of the compound (i.e., affinity, onset and duration of binding) and in particular should be based upon the recommendations and prescription of a qualified physician or veterinarian.

[0076] The compounds of the invention preferably have a long duration of action, which is important to facilitate dosing schedules. In rats, the present compounds have a 7-10 fold longer duration of action than cocaine (Fleckenstein et al, “Highly potent cocaine analogs cause long-lasting increases in locomotor activity,” Eur. J. Pharmacol., in press, which is incorporated herein by reference in its entirety). In addition, the present compounds also preferably have a slow rate of entry into the brain, which is important in decreasing the potential for abuse (Stathis et al, supra, which is incorporated herein by reference in its entirety). The present compounds enter the brain more slowly than cocaine.

[0077] The therapeutic compositions useful in practicing the therapeutic methods of this invention may include, in admixture, a pharmaceutically acceptable excipient (carrier) and one or more of the compounds of the invention, as described herein as an active ingredient.

[0078] The preparation of therapeutic compositions which contain such neuroactive compounds as active ingredients is well understood in the art. Such compositions may be prepared for oral adminstration, or as injectables, either as liquid solutions or suspensions, however, solid forms suitable for solution in, or suspension in, liquid prior to injection can also be prepared. The preparation can also be emulsified. The active therapeutic ingredient is often mixed with excipients which are pharmaceutically acceptable and compatible with the active ingredient. Suitable excipients are, for example, water, saline, dextrose, glycerol, ethanol, or the like and combinations thereof. In addition, if desired, the composition can contain minor amounts of auxiliary substances such as wetting or emulsifying agents, and pH buffering agents which enhance the effectiveness of the active ingredient. The compounds of the invention can be formulated into the therapeutic composition as neutralized pharmaceutically acceptable salt forms.

[0079] The therapeutic compositions are conventionally administered orally, by unit dose, for example. The term “unit dose” when used in reference to a therapeutic composition of the present invention refers to physically discrete units suitable as unitary dosage for humans, each unit containing a predetermined quantity of active material calculated to produce the desired therapeutic effect in association with the required diluent; i.e., carrier, or vehicle.

[0080] The compositions are administered in a manner compatible with the dosage formulation, and in a therapeutically effective amount. The quantity to be administered depends on the subject to be treated, the presence of other agonists and antagonists in the subject's system, and degree of binding or inhibition of binding desired. Precise amounts of active ingredient required to be administered depend on the judgment of the practitioner and are peculiar to each individual. However, suitable dosages may range from about 0.01 to about 1000, preferably about 0.25 to about 500, and more preferably 10 to 50 milligrams of active ingredient per kilogram body weight of individual per day and depend on the route of administration. However, the exact dosage must be determined by factoring in rate of degradation in the stomach, absorption from the stomach, other medications administered, etc. Suitable regimes for administration are also variable, but are typified by an initial administration followed by repeated doses at one or more hour intervals by a subsequent injection or other administration. Alternatively, continuous intravenous infusion sufficient to maintain appropriate concentrations in the blood are contemplated.

[0081] The compounds of the present invention may be administered for their activities as surrogate agonist medications for cocaine, nicotine, alcohol, amphetamine and other psychostimulant abuse. Because of their favorable binding characteristics to transporters of neurotransmitters, they may be used for inhibiting the uptake of dopamine, norepinephrine, serotonin and other monoamines. The compounds of the present invention may find use as antipsychotics, antidepressants, local anesthetics, anti-Parkinsonian agents, anti-obesity drugs, drugs useful in the treatment of bipolar disorder, eating disorders, obesity, attention deficit disorder, panic attacks and disorder, obsessive-compulsive disorder, sexual dysfunction, as anticholinergic agents and as sigma receptor drugs.

[0082] The compounds of the invention may also be useful in treating neurodegenerative disorders, in particular for treating Parkinson's Disease, but also may be useful in the treatment of cocaine, nicotine and alcohol addiction.

[0083] The preferred compounds of the present invention are derived from the series of compounds designated RTI-4229. The physical properties of some of these compounds are given in Table I. TABLE 1 Physical Properties of 2β-substituted Heterocyclic Analogs of 3β-(4-Substituted-phenyl) Tropane and Cocaine Code Molecular [α]D Yield Name Formulae^(a)    mp° C. (c) MeOH % RTI-188 C₂₂H₂₃Cl₂N₃O^(e)    160-162  +84.59 (0.36) 42 RTI-195 C₂₃H₂₆CN₃O^(e)    175-178  +97.22 (0.25) 40 RTI-194 C₁₈H24_(CN)3₀ ^(d)    146 (dec)  −43.05 (0.15) 58 RTI-200 C₂₂H₂₃Cl₂N₃S^(e)    165-170  −42.81 (0.16) 58 RTI-199 C₂₃H₂₆CN₃S^(d)    180-185  −33.50 (0.20) 58 RTI-189 C₂₇H₂₉CN₂O₇ ^(b,e)    126 (dec) +101.43 (0.21) 49 RTI-178 C₂₉H₃₂N₂O₇ ^(b,f)    175-181 −104.04 (0.60) 72 RTI-219 C₂₃H₂₄CN₂S^(f)    228-230  +27.43 (0.11) 30 RTI-202 C₂₁H₂₂Cl₂N₂S^(c)    140-150 (dec) −172.49 (0.28) 41 RTI-161 C₁₅H₁₈Cl₂N₂ ^(e)  >220 (dec)  −71.00 (0.50) 77 RTI-158 C₁₆H₂₁CN₂    270 (dec)  −76.40 (0.50) 67 RTI-163 C₁₅H₁₈CN₅ ^(e)    296-300 −124.94 (0.39) 33 RTI-157 C₁₆H₂₃Cl₂N₅ ^(c)  <212 (dec) −110.97 (0.16) 88 RTI-165 C₁₈H₂₂Cl₂N₂O    235 (dec) −102.89 (0.46) 46 RTI-171 C₁₉H₂₅CN₂O    277 −107.28 (0.71) 62 RTI-180 C₁₈H₂₂CN₂O^(c)  <235 (dec)  −94.57 (0.39) 49 RTI-177 C₂₃H₂₄Cl₂N₂O^(c)    287  −97.50 (0.28) 50 RTI-176 C₂₄H₂₇CN₂O    270-295 (dec) −102.22 (0.68) 77 RTI-181 C₂₃H24_(CN2)O₃ ^(d) <2679 (dec)  −91.11 (0.43) 56 RTI-184 C₁₉H₂₃CN₂O₃ ^(d)    117-121  −53.60 (0.25) 82 RTI-185 C₂₄H₂₅CN₂O₃    205  −56.71 (0.43) 68

[0084] Many of the preferred compounds of the invention fall within the broad class of compounds described by the formula:

[0085] wherein Y=CH₂R₃, CO₂R₂, CONRR¹,

[0086] R₁=hydrogen, C₁₋₅ alkyl,

[0087] R₂=hydrogen, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₆alkynyl, halogen, amine, CH₂C₆H₅, (CH₂)₂C₆H₅, (CH₂)₃C₆H₅ or

[0088] R₃=OH, hydrogen, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, Cl, Br, I, CN, NH₂, NHC₁₋₆ alkyl, NC₁₋₆ alkyl, OCOC₁₋₆ alkyl, OCOC alkylaryl,

[0089] A=S, O or N

[0090] X=H, C₁₋₆ alkyl, C₃₋₈ cycloalkyl, C₁₋₄ alkoxy, C₁₋₆ alkynyl, halogen, amino, acylamido, C₂H₅, CH₂CH₃CH₃, CH(CH₃)₂₁ Z=H, I, Br, Cl, F, CN, CF₃, NO₂, N₃, OR₁, CONH₂, CO₂R,, C₁-6 alkyl, NR₄R₅, NHCOR₅, NHCO₂R₆, and Q¹ and Q² may be the same or different and =H, OCH₃, or Cl,

[0091] wherein R₄-R₆ are each C₁₆ alkyl, R and R¹ are independently H, C₁₋₆ alkyl, C₁₆ alkene, C₁₆ alkyne, phenyl, phenyl substituted with 1-3 of C₁₆ alkyl, alkene, alkyl or alkoxy, C₁₆ alkoxy, phenoxy, amine, amine substituted with 1-2 of C₁₆ alkyl, alkene, alkyne, alkoxy or phenyl or phenoxy or R and R¹ may combine to form heterocyclic structure including pyrrolidinyl, piperidinyl and morpholino moieties, unsubstituted or substituted with 1-2 C₁₋₆ alkyl, alkene, alkyne or alkoxy groups.

[0092] The present inventors have surprisingly found that certain of the RTI-4229 series of compounds are particularly potent pharmaceutical agents in accordance with the present invention.

[0093] Preferred compounds of the RTI-4229 series include the following: RTI-4229-31, 32, 51, 55, 83, 96, 97, 98, 101, 105, 108, 110, 111, 112, 116, 121, 122, 123, 127, 132, 139, 140, 142, 145, 146, 147, 150, 153, 173, 178, 188, 189, 190, 191, 193, 195, 199, 200, 203, 204, 205, 206, 214, 219, 230, 239, 240, 241, 242, 243, 251, 252, 274, 277, 278, 279, 280, 281, 282, 283, 286, 287, 296, 304, 305, 307, 309, 318, 330 and 422. The chemical structures of these compounds, along with their IC₅₀ values for inhibition of radioligand binding are given below. DA is dopamine, 5-HT is 5-hydroxytryptamine (serotonin), and NE is norepinephrine, DA=[³H]WIN 35,428; 5-HT [³H] paroxetine and NE_(N)[³H] nisofetine: RTI-4229-31 DA 1.12 ± 0.1 5-HT 44.5 ± 1.34 NE_(N) 37 ± 2.1

RTI-4229-32 DA 1.71 ± 0.31 5-HT 240 ± 27 NE_(N) 60 ± 0.53

RTI-4229-51 DA 1.69 ± 0.23 5-HT 240 ± 0.24 NE_(N) 37.4 ± 5.2

RTI-4229-55 DA 1.26 ± 0.04 5-HT 4.21 ± 0.34 NE_(N) 36 ± 3

RTI-4229-83 DA 55 ± 2 5-HT 28.4 ± 3.83 NE_(N) 4.027.87 ± 380.70

RTI-4229-96 DA 2.95 ± 0.58 5-HT 76 ± 2.8 NE_(N) 520 ± 10.4

RTI-4229-97 DA 3.91 ± 0.59 5-HT 181 ± 14 NE_(N) 282 ± 30

RTI-4229-98 DA 0.69 ± 0.2 5-HT 0.36 ± 0.047 NE_(N) 10.97 ± 0.88

RTI-4229-101 DA 2.2 ± 0.19 5-HT 26 ± 3.2 NE_(N) ±

RTI-4229-105 DA 1.60 ± 0.05 5-HT 1.43 ± 25 NE_(N) 127.2 ± 5.9

RTI-4229-108 DA 2.64 ± 0.31 5-HT 98 ± 8.7 NE_(N) 129.3 ± 15

RTI-4229-110 DA 0.62 ± 0.09 5-HT 4.13 ± 0.62 NE_(N) 5.45 ± 0.21

RTI-4229-111 DA 0.79 ± 0.08 5-HT 3.13 ± 0.36 NE_(N) 17.96 ± 0.85

RTI-4229-112 DA 0.82 ± 0.05 5-HT 10.5 ± 0.41 NE_(N) 36.2 ± 1.02

RTI-4229-116 DA 33 ± 3.9 5-HT 1.227 ± 176 NE_(N) 967.55 ± 26.25

RTI-4229-121 DA 0.43 ± 0.05 5-HT 55.84 ± 6.53 NE_(N) 285 ± 7.6

RTI-4229-122 DA 1.50 ± 0.35 5-HT 184.38 ± 21.91 NE_(N) 3.791 ± 149

RTI-4229-123 DA 1.78 5-HT 3.53 NE_(N) 393

RTI-4229-127 DA 19 ± 1 5-HT 4.499 ± 557 NE_(N) 3.444 ± 44

RTI-4229-132 DA 3.48 ± 0.11 5-HT 208 ± 18 NE_(N) 137.3 ± 10.5

RTI-4229-139 DA 1.67 ± 0.13 5-HT 85 ± 9.3 NE_(N) 56.9 ± 2.6

RTI-4229-140 DA 101 ± 16 5-HT 5.701 ± 721 NE_(N) 2.076 ± 285

RTI-4229-142 DA 4.39 ± 0.20 5-HT 68.59 ± 2.02 NE_(N) 18.78 ± 0.68

RTI-4229-145 DA 9.60 ± 0.42 5-HT 2.932 ± 181 NE_(N) 1.478 ± 96

RTI-4229-146 DA 2.05 ± 0.23 5-HT 98 ± 10 NE_(N) 144 ± 3

RTI-4229-147 DA 1.38 ± 0.03 5-HT 12.393.99 ± 1207.03 NE_(N) 3.949 ± 72

RTI-4229-150 DA 3.74 ± 0.52 5-HT 2.019 ± 133 NE_(N) 4.738 ± 322

RTI-4229-153 DA 1.06 ± 0.12 5-HT 3.59 ± 0.27 NE_(N) 132 ± 5

RTI-4229-173 DA 49.9 ± 7.3 5-HT 8.13 ± 0.30 NE_(N) 122 ± 12

RTI-4229-178 DA 35.4 ± 1.74 5-HT 1.698.77 ± 166.68 NE_(N) 677 ± 67.5

RTI-4229-188 DA 12.56 ± 1.03 5-HT 3.303.76 ± 195.85 NE_(N) 929 ± 88.1

RTI-4229-189 DA 19.71 ± 1.98 5-HT 1.116.18 ± 107.148 NE_(N) 496 ± 42.1

RTI-4229-190 DA 0.96 ± 0.10 5-HT 168 ± 1.8 NE_(N) 235 ± 8.39

RTI-4229-191 DA 0.61 ± 0.08 5-HT 15.5 ± 0.72 NE_(N) 101.7 ± 10.5

RTI-4229-193 DA 1.68 ± 0.14 5-HT 1.066.38 ± 109.12 NE_(N) 544 ± 27.7

RTI-4229-195 DA 47.48 ± 4.76 5-HT 22.310.9 ± 822.83 NE_(N) 1.310 ± 36.7

RTI-4229-199 DA 35.88 ± 3.40 5-HT 51.459.7 ± 4.513.10 NE_(N) 24.320.8 ± 3.822.61

RTI-4229-200 DA 15.29 ± 2.43 5-HT 18.416.5 ± 1.508.79 NE_(N) 4.142.08 ± 466.07

RTI-4229-203 DA 9.37 ± 0.52 5-HT 2.153.39 ± 143.18 NE_(N) 2.743.73 ± 140.92

RTI-4229-204 DA 3.91 ± 0.23 5-HT 3.772.17 ± 383.64 NE_(N) 4.782.70 ± 487.10

RTI-4229-205 DA 8.19 ± 0.90 5-HT 5.237.30 ± 453.397 NE_(N) 2.136.62 ± 208.52

RTI-4229-206 DA 27.38 ± 1.47 5-HT 1.203.39 ± 41.79 NE_(N) 1.277.60 ± 117.68

RTI-4229-214 DA 2.90 5-HT 88,800 NE_(N) 8550

RTI-4229-219 DA 5.71 ± 0.36 5-HT 10.341 5 ± 76.11 NE_(N) 8.563 ± 824

RTI-4229-230 DA 1.26 ± 0.17 5-HT 57.41 ± 5.04 NE_(N) 141 ± 16.1

RTI-4229-239 DA 0.61 ± 0.07 5-HT 114.3 ± 3.69 NE_(N) 35.6 ± 2.57

RTI-4229-240 DA 1.38 ± 0.03 5-HT 38.4 ± 2.31 NE_(N) 84.5 ± 3.09

RTI-4229-241 DA 1.02 ± 0.06 5-HT 618.5 ± 28 NE_(N) 124 ± 3.56

RTI-4229-242 DA 7.57 ± 0.31 5-HT 226.54 ± 27.37 NE_(N) 510.1 ± 51.4

RTI-4229-243 DA 129 ± 19.6 5-HT 155.93 ± 15.27 NE_(M) ±NE_(N) 540 ±

RTI-4229-251 DA 1.93 ± 0.14 5-HT 10.1 ± 1.1 NE_(N) 114 ± 13.1

RTI-4229-252 DA 2.56 ± 0.22 5-HT 35.2 ± 2.45 NE_(N) 124.6 ± 8.3

RTI-4229-274 DA 3.96 ± 0.2 5-HT 5.62 ± 0.2 NE_(N) 14.4 ± 1.3

RTI-4229-277 DA 5.94 ± 0.61 5-HT 2.909.71 ± 255.41 NE_(N) 5.695.38 ± 214.72

RTI-4229-278 DA 8.14 ± 0.73 5-HT 2.146.50 ± 138.71 NE_(N) 4.095.01 ± 413.45

RTI-4229-279 DA 5.96 ± 0.48 5-HT 1.06 ± 0.10 NE_(N) 74.3 ± 3.8

RTI-4229-280 DA 3.12 ± 0.39 5-HT 6.81 ± 0.41 NE_(N) 484.13 ± 51.6

RTI-4229-281 BIH-141-7 DA 2.37 ± 0.28 5-HT 15.69 ± 1.5 NE_(N) 820.5 ± 45.8

RTI-4229-282 BIH-141-2 DA 68.53 ± 7.08 5-HT 70.38 ± 4.13 NE_(N) 3921.58 ± 130

RTI-4229-283 BIH-141-2 DA 14.35 ± 0.3 5-HT 3.13 ± 0.16 NE_(N) 3125 ± 333

RTI-4229-286 DA 20.7 ± 0.57 5-HT 5062 ± 485 NE_(N) 1231 ± 91

RTI-4229-287 DA 325 ± 20 5-HT 1686 ± 140 NE_(N) 17.819 ± 440

RTI-4229-296 BIH-141-1 DA 5.29 ± 0.53 5-HT 11.39 ± 0.28 NE_(N) 1592.23 ± 93.4

RTI-4229-304 BIH-141-11 DA 15.04 ± 1.2 5-HT 7.09 ± 0.71 NE_(N) 2799 ± 300

RTI-4229-305 BIH-141-18 DA 1.24 ± 0.11 5-HT 1.59 ± 0.2 NE_(N) 21.8 ± 1.0

RTI-4229-307 BIH-141-15 DA 6.11 ± 0.67 5-HT 3.16 ± 0.33 NE_(N) 115.8 ± 5.1

RTI-4229-309 BIH-141-17 DA 1.73 ± 0.05 5-HT 2.25 ± 0.17 NE_(N) 14.9 ± 1.18

RTI-4229-318 DA 0.51 ± 0.03 5-HT 0.80 ± 0.06 NE_(N) 21.1 ± 1.0

RTI-4229-330 DA 310.2 ± 21 5-HT 15.1 ± 0.97 NE_(N) ±

RTI-4229-422 DA 1.96 5-HT 1,100 NE_(N) 6090

[0094] Particularly preferred compounds include RTI-4229-77, 87, 113, 114, 117, 119, 120, 124, 125, 126, 130, 141, 143, 144, 151, 152, 154, 165, 171, 176, 177, 180, 181, 194, 202, 252, 295, 298, 319, 334, 335, 336, 337, 338, 345, 346, 347, 348, 352 and 353. The chemical structures of these compounds are given below: RTI-4229-77 DA 2.51 ± 0.25 5-HT ±NE_(N) 2.246.86 ± 238.99

RTI-4229-87 DA 204 ± 29 5-HT 28.391 ± 2.324 NE_(N) 35.782 ± 6.245

RTI-4229-113 DA 1.98 ± 0.05 5-HT 2.3336 ± 176 NE_(N) 2.955 ± 223

RTI-4229-114 DA 1.40 ± 0.13 5-HT 1.404 ± 7.1 NE_(N) 778 ± 21

RTI-4229-117 DA 6.45 ± 0.85 5-HT 6.090 ± 488 NE_(N) 1.926 ± 38

RTI-4229-119 DA 167 ± 13 5-HT 40.615 ± 9.416 NE_(N) 6.985 ± 635

RTI-4229-120 DA 3.26 ± 0.06 5-HT 24.47 ± 1.515 NE_(N) 5.833 ± 373

RTI-4229-124 DA 1.028 ± 65 5-HT 33.085 ± 5.434 NE_(N) 70.993 ± 3.563

RTI-4229-125 DA 4.05 ± 0.57 5-HT 2.584 ± 799 NE_(N) 363 ± 36

RTI-4229-126 DA 100 ± 6.3 5-HT 3.824 ± 418 NE_(N) 7.876 ± 551

RTI-4229-130 DA 1.62 ± 0.02 5-HT 195 ± 4.8 NE_(N) 245 ± 13

RTI-4229-141 DA 1.81 ± 0.19 5-HT 337 ± 43 NE_(N) 835 ± 7.5

RTI-4229-143 DA 4.1 ± 0.22 5-HT 404 ± 58 NE_(N) 4.069 ± 177

RTI-4229-144 DA 3.44 ± 0.36 5-HT 106 ± 10 NE_(N) 1.825 ± 166

RTI-4229-151 DA 2.33 ± 0.26 5-HT 1.074 ± 125 NE_(N) 60 ± 2

RTI-4229-152 DA 494 ± 37 5-HT 1.995 ± 109 NE_(N) 22.689 ± 1.957

RTI-4229-154 DA 6.0 ± 0.55 5-HT 3.460 ± 245 NE_(N) 135 ± 13

RTI-4229-165 DA 0.59 ± 0.04 5-HT 572 ± 58 NE_(N) 161 ± 12

RTI-4229-171 DA 0.93 ± 0.09 5-HT 3.818.25 ± 346.14 NE_(N) 254 ± 31

RTI-4229-176 DA 1.58 ± 0.02 5-HT 5.109.72 ± 187.101 NE_(N) 398 ± 17.6

RTI-4229-177 DA 1.28 ± 0.18 5-HT 2.418.21 ± 135.68 NE_(N) 504 ± 29

RTI-4229-180 DA 0.73 ± 0.04 5-HT 36.35 ± 4.99 NE_(N) 67.9 ± 5.25

RTI-4229-181 DA 2.57 ± 0.14 5-HT 100 ± 9.0 NE_(N) 868 ± 95

RTI-4229-194 DA 4.45 ± 0.12 5-HT 4.884.47 ± 155.42 NE_(N) 253 ± 18.9

RTI-4229-202 DA 1.37 ± 0.14 5-HT 1.118.85 ± 120.00 NE_(N) 402.8 ± 29.5

RTI-4229-295 BIH 141-4 DA 21.31 ± 0.87 5-HT 2.96 ± 0.04 NE_(N) 1349 ± 105

RTI-4229-298 BIH-141-4 DA 3.7 ± 0.16 5-HT 46.8 ± 5.8 NE_(N) 346.6 ± 25

RTI-4229-319 DA 1.1 ± 0.09 5-HT 11.4 ± 1.3 NE_(N) 70.2 ± 6.28

RTI-4229-334 DA 0.50 ± 0.03 5-HT 3086 ± 153 NE_(N) 120 ± 10.4

RTI-4229-335 DA 1.19 ± 0.12 5-HT 2318 ± 153 NE_(N) 954 ± 97.3

RTI-4229-336 DA 4.09 ± 0.44 5-HT 5741 ± 421 NE_(N) 1714 ± 38.5

RTI-4229-337 DA 7.31 ± 0.61 5-HT 36.842 ± 3616 NE_(N) 6321 ± 703

RTI-4229-338 DA 1104.2 ± 54.6 5-HT 7.41 ± 0.55 NE_(N) 3366 ± 584

RTI-4229-345 DA 6.42 ± 0.46 5-HT > 76.000 ±NE_(N) 5290.4 ± 448.99

RTI-4229-346 DA 1.57 ± 0.10 5-HT 5880 ± 179 NE_(N) 762.01 ± 37.8

RTI-4229-347 DA 1.86 ± 0.09 5-HT 7256.95 ± 210 NE_(N) 918.4 ± 108.34

RTI-4229-348 DA 28.2 ± 1.9 5-HT 34.674 ± 3954 NE_(N) 2667.2 ± 6267.3

RTI-4229-352 DA 2.86 ± 0.21 5-HT 64.9 ± 1.97 NE_(N) 52.4 ± 4.9

RTI-4229-353 DA 330.54 ± 17.12 5-HT 0.69 ± 0.07 NE_(N) 148.4 ± 9.15

[0095] It should be noted that compound RTI-353 is a highly potent compound at the serotonin site, and is selective relative to the dopamine and norepinephrine sites. This compound is particularly useful as an antidepressant, and as an imaging agent for serotonin transporters.

[0096] Having generally described this invention, a further understanding can be obtained by reference to certain specific examples which are provided herein for purposes of illustration only and are not intended to be limiting unless otherwise specified.

EXAMPLES

[0097] All certified grade reagents or solvents were purchased from Aldrich Chemical Co. or Fluka Chemical Co. All reagents were normally used without further purification. When anhydrous conditions were required, solvents were distilled and dried by standard techniques immediately prior to use.

[0098] All air and moisture sensitive reactions were conducted under a prepurified nitrogen atmosphere in flame-dried glassware, previously dried at 150° C. Anhydrous solvents were transferred using conventional syringe or steel canula techniques under an inert atmosphere. Removal of solvents in vacuo was done on a Buchi rotavapor rotary evaporator operated at water aspirator pressure. temperature and then at high vacuum to remove residual traces of oxalyl chloride. The resulting residue of acid chloride was suspended in 5 ml methylene chloride under nitrogen at 0° C., and 2.0 eq of the amine hydrochloride containing 4.0 eq of triethylamine, or 2.5 eq of the amine free base was added. The mixture was stirred at room temperature overnight. Aqueous 3N NaOH (5 ml) was added to basify the reaction mixture, the organic layer was separated and the aqueous layer extracted with 3×10 ml chloroform. The combined organic layers were dried (Na₂SO₄), filtered and the solvent removed in vacuo to give crude product. The crude was purified by flash column chromatography or crystallization.

EXAMPLE 2

[0099] 3β-(4-Chlorophenyl)-2P-(5-phenyl-1,3,4-oxadiazol-2-yl)-tropane Hydrochloride (RTI-188)

[0100] To a solution of 0.59 g (2 mmol) of 3β-(4-Chlorophenyl)-tropane-2β-carboxylic acid (chloro acid) in 2 ml of POCl₃ was added 0.31 g (2.2 mmol) of N-benzoic hydrazide and refluxed under nitrogen for 2 hours. The reaction mixture was cooled, poured into ice and rendered basic to pH 7-8 using concentrated NH₄0H. To the ice cold aqueous layer was added 10 ml brine and extracted thrice with 10 ml methylene chloride. The organic layers were combined dried (NaSO₄), filtered, and

[0101]¹H NMR and 13C NMR spectra were recorded at 250 Mhz on a Bruker AM250 spectrometer. Optical rotations were recorded on at the Sodium D line on a Rudolph Research Autopol III polarimeter (1 dm cell). Melting point was recorded on a Uni-melt Thomas Hoover capillary melting point apparatus in open capillary tubes and were uncorrected. Elemental analysis were performed by Atlantic Microlab, Inc., Norcross, Ga.

[0102] Reaction products were purified by flash column chromatography using silica gel (mesh size 230-400) purchased from VWR Scientific. Thin layer chromatography (TLC) was performed on Whatman 254 nm fluorescent silica gel GOA (1×3 inches, 250 [μm thickness]) precoated TLC plates using the solvent systems indicated. Developed chromatograms were evaluated under 254 nm UV light or with iodine.

EXAMPLE 1

[0103] General Procedure For the Preparation of Amides

[0104] To a solution of 1 mmol of 3β-(4-Chlorophenyl)-tropane-2β-carboxylic acid or 3β-(4-Methylphenyl)-tropane-2β-carboxylic acid in 5 ml of methylene chloride was added dropwise with stirring under nitrogen 2.0 eq oxalyl chloride (2 M solution in methylene chloride). The resulting solution was stirred at room temperature for an hour after evolution of gas has ceased. The solvent was removed in vacuo at room the solvent removed in vacuo to give 0.9 g of crude residue. Purification of the residue by flash column chromatography [50% (ether/triethylamine 9:1) in hexane] gave 0.33 g (42%) of pure oxadiazole (RTI-188) which was recrystallized from ether/petroleum ether: ¹H NMR (CDCl₃) 1.81 (m, 3H), 2.18 (s, 3 H), 2.26 (m, 2H), 2.66 (m, 1H), 3.33 (m, 2H), 3.51 (m, 2 H), 7.16 (m, 4H) 7.45 (m, 3H), 7.86 (m, 2H); IR (CHCl₃) 2950, 1550, 1490, 1450, 1340, 1090 cm⁻¹; [β]_(D)−106.250 (c=0.08, CHCl₃)

[0105] The oxadiazole was converted into hydrochloride salt: ¹H NMR (MeOD) 2.08 (m, 1H), 2.57 (m, 5H), 3.0 (s, 3H), 4.01 i (m, 2H), 4.15 (m, 1H), 4.39 (m, 1H), 7.24 (m, 4H), 7.52 (m, 5H): mp 160-162° C.; Anal calcd for C₂₂H₂₃Cl₂N₃O.0.75H₂O; C=61.47; H=5.74, N=9.78; Cl=16.50; found C=61.47, H=5.73, N=9.76; Cl=16.56; [α]_(D)+84.59° (c=0.36, CH₃OH).

[0106] Further elution gave as a second fraction 0.1 g (13w) of white solid which was characterized to be 3X-(4-Chlorophenyl)-2(-(5-phenyl-1,3,4-oxadiazol-2-yl)-tropane: ¹H NMR (CDCl₃) 1.76 (m, 3H), 2.06 (s, 3H), 2.45 (s, 3H), 3.36 (m, 2H), 3.51 (m, 1H), 3.65 (m, 1H), 7.21 (m, 4H), 7.47 (m, 3H) 7.91 (m, 2H); mp 170-171° C.; Anal calcd for C₂₂H₂₂CIN₃O; C=69.55; H=5.84, N=11.06; Cl=9.33; found C=69.49, H=5.85, N=11.01; Cl=9.41; [α]_(D)+33.06° (c=0.18, CHCl₃)

EXAMPLE 3

[0107] 3β-(4-Methylphenyl)-2β-(5-phenyl-1,3,4-oxadiazol-2-yl)-tropane Hydrochloride (RTI-195)

[0108] Reaction of 0.65 g (2.5 mmol) of 3D-(4-Methylphenyl)-tropane-213-carboxylic acid (Methyl acid) as described above for RTI-188 gave after work-up and purification by flash column chromatography [(50% (ether/triethylamine 9:1 ) in hexane] 0.36 g (40%) of pure oxadiazole (RTI-195) which was recrystallized from ether/petroleum ether: ¹H NMR (CDCl₃) 1.83 (m, 3H), 2.18 (s, 3H), 2.21 (s, 3H), 2.3 (m, 2H), 2.67 (m, 1H), 3.33 (m, 1H), 3.41 (m, 1H), 3.53 (m, 1H), 3.61 (m, 1 H) 7.0 (m, 2H).7.13 (m, 2H), 7.44 (m, 3H), 7.86 (m, 2H); IR (CHCL₃) 2990, 1545, 1505, 1440, 1350. cm⁻¹; [α]_(D)−163.920 (c=0.2, CHCl₃)

[0109] The oxadiazole was converted into hydrochloride salt: H NMR (MeOD) 2.05 (m, 1H), 2.21 (s, 3H), 2.51 (m, 5H), 2.99 (s, 3H), 3.86 (m, 1H), 3.95 (m, 1H), 4.14 (m, 1H), 4.35 (m, 1H), 7.02 (m, 4H) 7.53 (m, 5H); mp 175-178° C.; Anal calcd for C₂₃H₂₆CIN₃O.0.75H₂O; C=67.47; H=6.77, N=10.26; Cl=8.66; found C=67.58, H=6.79, N=10.34; Cl=8.78; [α]_(D)+97.220 (c=0.25, CH₃OH).

[0110] Further elution gave as a second fraction 0.18 g (20%) of solid which was characterized to be 3β-(4-Methylphenyl)-2α-(5-phenyl-1,3,4-oxadiazol-2-yl)-tropane which was recrystallized from ether/petroleum ether: ¹H NMR (CDCl₃) 1.77 (m, 2H), 2.0 (m, 4H), 2.25 (s, 3H), 2.47 (s, 3H), 3.33 (m, 2H), 3.51 (m, 1H), 3.69 (d of d, J=2.6, 12 Hz, 1H), 6.91 (m, 2H) 7.03 (m, 2H).7.45 (m, 2H), 7.45 (m, 3H), 7.89 (m, 2H); IR (CHCL₃) 3020, 1540, 1510, 1415, 1250, 1215. cm; Anal calcd for C₂₃H₂₅N₃O; C=76.85; H=7.01, N=11.69; found C=76.60, H=7.12, N=11.55; [α]_(D)+40.730 (C=0.28, CHCl₃)

EXAMPLE 4

[0111] 3β-(4-Methylphenyl)-2β-(5-methyl-1,3,4-oxadiazol-2-yl)-tropane Hydrochloride (RTI-194)

[0112] Reaction of 0.65 g (2.5 mmol) of methyl acid as described above for RTI-195 using 0.21 g (2.75 mmol) of N-acetic hydrazide gave after work-up and Purification by flash column chromatography [(75%. (ether/triethylamine 9:1 ) in hexane] 0.29 g (39%) of pure oxadiazole (RTI-194) which was recrystallized from ether/petroleum ether: ¹H NMR (CDCl₃) 1.75 (m, 3H), 2.18 (s, 3H), 2.22 (s, 3H), 2.25 (m, 2H), 2.35 (s, 3H), 2.56 (m, 1H), 3.24 (m, 1H), 3.4 (m, 2H), 3.47 (m, 1H) 7.0 (m, 4H); ¹³C NMR (CDCl₃) 11.06, 20.9, 25.08, 26.32, 34.11, 34.6, 41.83, 45.73, 61.97, 66.21, 127.11, 128.85, 135.85, 138.19, 162.5, 167.44; IR (CHCL₃) 2950, 1590, 1510, 1450, 1350, 1215 cm⁻¹; [α]_(D)−108.470 (c=0.14, CHCl₃).

[0113] The oxadiazole was converted into hydrochloride salt: ¹H NMR (MeOD) 1.99 (m, 1H), 2.23 (s, 3H), 2.27 (s, 3H), 2.47 (m, 5H), 2.94 (s, 3H), 3.72 (m, 1H), 3.79 (m, 1H), 4.10 (m, 1H), 4.23 (m, 1H), 7.05 (m, 4H); mp 146° C.(dec); Anal calcd for Cl₈H₂₄CIN₃O.0.5H₂O; C=63.06; H=7.35, N=12.26; Cl=10.34; found C=63.21, H=7.40, N=12.07; Cl=10.27; [α]_(D)−43.05° (c=0.15, CH₃OH).

EXAMPLE 5

[0114] 3D-(4-Chlorophenyl)-213-(S-phenyl-1,3,4-thiadiazol-2-yl)-tropane Hydrochloride (RTI-200).

[0115] Reaction of 0.59 g (2 mmol) of 3β-(4-Chlorophenyl)tropane-2β-carboxylic acid as described above for the preparation of amides gave after purification of the crude by crystallizing from ethyl acetate/ether 0.52 g (66%) of pure N-[3p-(4-Chlorophenyl)-tropane-2β-carboxylic]-N′-benzoylhydrazide: ¹H NMR (CDCl₃) δ 1.76 (m, 3H), 2.24 (m, 2H), 2.41 (s, 3H) 2.51 (m, 1H), 2.68 (m, 1H), 3.18 (m, 1H), 3.44 (m, 2H), 7.22 (m, 4H), 7.46 (m, 3H), 7.78 (m, 2H), 9.02 (br s, 1H), 12.97 (br s, 1H); IR (CHCl₃) 3385, 3035, 3000, 1620, 1570, 1485, 1450, 1215 cm⁻¹.

[0116] A solution of 0.4 g (1 mmol) of N-[3D-(4-Chlorophenyl)-tropane-2β-carboxyic]-N′-benzoyl-hydrazide and 0.8 g (2 mmol) of Lawesson's reagent in 10 ml toluene was refluxed for 4 h under nitrogen. The reaction mixture was cooled and solvent removed in vacuo to give a yellow residue. To the residue was added 3 g of silica gel and 10 ml of methylene chloride, the resulting slurry was mixed properly and the solvent removed in vacuo. The crude compound impregnated on silica gel was loaded on a column and purified by flash column chromatography [50% ether/triethylamine(9:1) in hexane] to obtain 0.23 g (58%) of pure thiadiazole (RTI-200) which was further purified by recrystallizing from ether: ¹H NMR (CDCl₃) δ 1.75 (m, 3H), 2.20 (m, 3H), 2.32 (s, 3H), 3.30 (m, 3H), 3.78 (m, 1H), 6.86 (m, 2H), 7.08 (m, 2H), 7.43 (m, 3H), 7.97 (m, 2H); NMR 25.55, 25.88, 34.60, 36.09, 41.55, 49.73, 61.48, 65.33, 127.59, 128.28, 128.78, 128.88, 130.37, 130.88, 132.19, 139.27, 168-29, 169.56; IR (CC14) 2940, 1490, 1460, 1340, 1245, 1100, 1010 cm¹

[0117] The thiadiazole was converted into hydrochloride salt: ¹H NMR (MeOD) δ 2.06 (m, 1H), 2.53 (m, 5H), 2.97 (s, 3H), 3.92 (m, 1H), 4.17 (m, 2H), 4.39 (m, 1H), 7.11 (m, 2H), 7.26 (m, 2H), 7.51 (m, 3H), 7.79 (m, 2H); mp 165-170° C.; Anal calcd for C₂₂H₂₃Cl₂N₃S.0.75H₂O; C=59.26, H=5.54, N 9.42, Cl=15.90; S=7.19. found C=59.27, H=5.52, N=9.40, Cl=15.99; S 7.09; [°]_(D)−42.81° (c=0.16, MeOH).

[0118] Further elution gave 0.08 g (21%) as a second fraction which was characterized to be 3β-(4-chlorophenyl)-2α-(5-phenyl-1,3,4-oxadiazol-2-yl)-tropane.

EXAMPLE 6

[0119] 3β-(4-Methylphenyl)-2β-(5-phenyl-1,3,4-thiadiazol-2-yl)-tropane Hydrochloride (RTI-199) Reaction of 0.65 g (2.5 mmol) of 3p-(4-Methylphenyl)-tropane-2p-carboxylic acid as described above for preparation of amides gave after work up and purification by flash column chromatography [(50% CMA-80 in methylene chloride)] 0.48 g (51%) pure N-[3β-(4-Methylphenyl) Tropane-2β-carboxylic]-N′-benzoyl-hydrazide which was further purified by recrystallizing from ether/pet ether: ¹H NMR (CDCl₃) δ 1.75 (m, 3H), 2.20 (m, 2H), 2.27 (s, 3H), 2.42 (s, 3H), 2.51 (m, 1 H), 2.67 (m, 1H), 3.18 (m, 1H), 3.47 (m, 2H), 7.11 (m, 4 H), 7.48 (m, 3H), 7.81 (m, 2H), 9.06 (br s, 1H), 13.09 (br s, 1H); IR (CHCl₃) 3385, 3045, 1625, 1570, 1460, 1420, 1100 cm⁻¹;

[0120] Reaction of 0.29 g (0.75 mmol) of N-[3β-(4-Methylphenyl)-tropane-2β-carboxyic]-N′-benzoyl-hydrazide as described above for RTI-200 gave after work and purification by flash chromatography [40% ether/triethylamine(9 : 1) in hexane] 0.16 g (58%) of pure thiadiazole (RTI-199): ¹H NMR (CDCl₃) δ 1.70 (m, 1H), 1.88 (m, 2H), 2.20 (s, 3H), 2.23 (m, 2H), 2.21 (s, 3H), 2.38 (m, 1H), 3.21 (m, 1H), 3.32 (m, 1H), 3.39 (m, 1H), 3.78 (m, 1H), 6.81 (m, 2H), 6.92 (m, 2H), 7.43 (m, 3H), 7.97 (m, 2H); ¹³C NMR 20.98, 25.65, 25.95, 34.79, 36.25, 41.65, 50.05, 61.68, 65.49, 127.32, 127.65, 128.89, 128.95, 130.29, 131.11, 135.94, 137.68, 168.83, 169.45; IR (CCl₄) 2935, 1510, 1450, 1250, 1120, 1100, 1060 cm⁻¹

[0121] The thiadiazole was converted into hydrochloride salt; ¹H NMR (MeOD) δ 1.95 (m, 1H), 2.17 (s, 3H), 2.41 (m, 5H), 2.89 (s, 3H), 3.76 (m, 1H), 4.05 (m, 2H), 4.30 (m, 1H), 4.22 (m, 1H), 6.89 (m, 2H), 6.99 (m, 2H), 7.39 (m, 3H), 7.67 (m, 2H); mp 180-185° C.; Anal calcd for C₂₃H₂₆CIN₃S.H₂O; C=65.62, H=6.46, N=9.98, Cl=18.42; S=7.62. found C=65.57, H=6.63, N=9.91, Cl=18.24; S=7.55; [α]_(D)−33.5° (c=0.2, MeOH)

[0122] Further elution gave 0.04 g (15%) of a second fraction which was characterized to be 3β-(4-Methylphenyl)-2α(5-phenyl-1,3,4-oxadiazol-2-yl)-tropane.

EXAMPLE 7

[0123] 3β-(4-Chlorophenyl)-2β-(5-phenyl-oxazol-2-yl)-tropane Tartrate RTI-189)

[0124] Reaction of 0.73 g (2.5 mmol) of 35-(4-Chlorophenyl)-tropane-2carboxylic acid as described above for the preparation of amides gave after purification by flash column chromatography (15% CMA 80 in methylene chloride) 0.8 g (81%) of pure 3β-(4-Chlorophenyl)-tropane-2β-N-(phenyacyl)carboxamide: ¹H NMR (CDCl₃) δ 1.71 (m, 3H), 2.19 (m, 2H), 2.39 (5, 3H), 2.46 (m, 1H), 2.58 (m, 1H), 3.13 (m, 1H), 3.43 (m, 2H), 4.74 (m, 2H), 7.13 (m, 4H), 7.49 (m, 2H), 7.59 (m, 1H), 7.96 (m, 2H), 10.57 (br s, 1H); IR (CHCl₃) 3135, 3010, 2930, 1695, 1650, 1590, 1530, 1485, 1450, 1355, 1220 cm¹.

[0125] A solution of 0.725 g (1.83 mmol) of 3β-(4-Chlorophenyl)-tropane-2p-N(phenyacyl)carboxamide in 6 ml POCl₃ was heated at 1250C under nitrogen for 2 hours. The reaction mixture was cooled and poured into ice and rendered basic to pH 7-8 using concentrated NH₄OH. To the ice cold aqueous layer was added 10 ml brine and extracted thrice with 10 ml methylene chloride. The organic layers were combined dried (NaSO₄), filtered, and the solvent removed in vacuo to 0.63 g crude oxazole. Purification of the crude by flash column chromatography [(40% (ether/triethylamine 9:1 ) in hexane] gave 0.34 g (49%) of pure oxazole (RTI-189) which was further purified by recrystallizing from ether/petroleum ether: ¹H NMR (CDCl₃) 1.79 (m, 3H), 2.22 (s, 3H), 2.27 (m, 2H), 2.66 (m, 1H), 3.27 (m, 1H), 3.40 (m, 2H), 3.53 (m, 1H), 7.11 (s, 1H), 7.16 (s, 4H) 7.31 (m, 5H); IR (CHCl₃) 2950, 1540, 1490, 1445, 1350, 1120, 1090 CM⁻¹; [α]_(D)−70.37° (c=0.19, CHCl₃)

[0126] The oxazole was converted into tartrate salt: ¹H NMR (MeOD) 2.14 (m, 1H), 2.54 (m, 5H), 2.96 (s, 3H), 3.75 (m, 2 H), 4.12 (m, 1H), 4.25 (m, 1H), 4.41 (s, 2H), 7.05 (m, 2 H), 7.29 (m, 7H), 7.45 (s, 1H), 7.43 (s, 1H); mp 126° C. (dec); Anal calcd for C₂₇H₂₉CIN₂O₇.0.75H₂O; C=59.78; H=5.67, N=5.16; Cl=6.54; found C=59.78, H=5.58, N=4.93; Cl=6.31; [α]_(D)+101.43° (c=0.21, CH₃OH)

EXAMPLE 8

[0127] 3β-(4-Methylphenyl)-2p-(5-phenyl-oxazol-2-yl)-tropane Tartrate (RTI-178)

[0128] Reaction of 0.52 g (2 mmol) of 3β-(4-Methylphenyl)-tropane-2β-carboxylic acid as described above for preparation of amides gave after work up and purification by flash column chromatography (15% CMA in methylene chloride) 0.54 g (72%) of pure 3p-(4-Methylphenyl)-tropane-2β-N-(phenyacyl)carboxamide: ¹H NMR (CDCl₃) δ 1.73 (m, 3H), 2.14 (m, 2H), 2.26 (s, 3H), 2.40 (s, 3H), 2.47 (m, 1H), 2.59 (m, 1H), 3.14 (m, 1H), 3.42 (m, 2H), 4.74 (m, 2H), 7.05 (m, 4H), 7.48 (m, 2H), 7.59 (m, 2H), 7.97 (m, 2H), 10.62 (br s, 1H); IR (CHCl₃) 3155, 3005, 2930, 1690, 1650, 1520, 1450, 1355, 1215 cm⁻¹

[0129] Reaction of 0.5 g (1.33 mmol) of 3D-(4-Methylphenyl)-tropane-2β-N-(phenyacyl)carboxamide as described above for RTI-189 gave after workup and purification by flash column chromatography [(40% (ether/triethylamine 9:1 ) in hexane] 0.1 g (31%) RTI-158 as a first fraction. Further elution gave 0.19 g (42%) of pure oxazole RTI-178: ¹H NMR (CDCl₃) 1.8 (m, 3 H), 2.18 (m, 2H), 2.21 (s, 3H), 2.22 (s, 3H), 2.67 (7n 1 H), 3.28 (m, 1H), 3.42 (m, 2H), 3.53 (m, 1H), 6.98 (m, 2 H), 7.11 (m, 3H), 7.30 (m, 5H).

[0130] The oxazole was crystallized as the tartrate salt: ¹H NMR (MeOD) 1.99 (m, 1H), 2.19 (s, 3H), 2.54 (m, 5H), 2.95 (s, 3 H), 3.74 (m, 2H), 4.13 (m, 1H), 4.26 (m, 1H), 4.4 (s, 2H), 6.91 (m, 2H), 7.0 (m, 2H), 7.25 (m, 2H), 7.33 (m, 3H), 7.43 (s, 1H); mp 175-181 C; Anal calcd for C₂₈H₃₂N₂O₇.1H₂O; C=63.87; H=6.51, N=5.32; found C=64.21, H=6.40, N=5.19; [α]_(D)−104.04° (c=0.6, CH₃OH)

EXAMPLE 9

[0131] 3β-(4-Chlorophenyl)-2β-(5-phenylthiazol-2-yl)-tropane Hydrochloride (RTI-219)

[0132] To a solution of 0.74 g (1.86 mmol) of 3β-(4-Chlorophenyl)-tropane-2β-N-(phenyacyl)carboxamide and 1.51 g (7.45 mmol) of Lawesson's reagent in 18 ml of toluene was refluxed under N₂ for 5 hours. The reaction mixture was cooled and solvent removed in vacuo to give crude residue. To the residue was added 3 g of silica gel and 10 ml of methylene chloride, the resulting slurry was mixed properly and the solvent removed in vacuo. The crude compound impregnated on silica gel was loaded on a column and purified by flash column chromatography [(40% (ether/triethylamine 9:1 ) in hexane] to give 0.21 g (30%) of pure thiazole RTI-219: ¹H NMR (CDC) 1.61 (m, 1H), 1.82 (m, 2H), 2.22 (m, 2H), 2.34 (s, 3H) 2.39 (m, 1H), 3.28 (m, 2H), 3.39 (m, 1H), 3.49 (m, 1H), 6.8 (m, 2H) 7.07 (m, 2H), 7.32 (m, 3H), 7.57 (m, 2H), 7.60 (s, 1H); ¹³C NMR (MeOD) 25.51, 25.99, 35.01, 36.92, 41.72, 52.97, 61.58, 65.70, 126.45, 127.60, 128.13, 128.89, 129.05, 131.91, 132.43, 136.11, 139.91, 140.27, 168.97; IR (CHCl₃) 2945, 1590, 1485, 1445, 1350, 1125, 1090. cm⁻¹.

[0133] The thiazole was converted into hydrochloride salt: ¹H NMR (MeOD) 1.99 (m, 1H), 2.51 (m, 5H), 2.93 (s, 3H), 3.79 (m, 2 H), 4.15 (m, 1H), 4.28 (m, 1H), 7.02 (d, J=8.5 Hz, 2H) 7.21 (d, J=8.5 Hz, 2H), 7.39 (m, 5H), 8.06 (s, 1H); mp 228-230° C.; Anal calcd for C₂₃H₂₄CIN₂S.H₂O; C=61.47, H=5.83, N=6.23, S=7.13, Cl=15.78; found C=61.61, H=5.76, N=6.20, S=7.51, Cl=15.84; [α]_(D)+27.43° (c=0.11, CH₃OH)

EXAMPLE 10

[0134] 3β-(4-Chlorophenyl)-2β-(benzothiazol-2-yl)-tropane Hydrochloride (RTI-202)

[0135] Reaction of 0.59 g (2 mmol) of 3β-(4-Chlorophenyl)-tropane-2β-carboxylic acid as described above for preparation of amides gave after purification of the crude by flash column chromatography (50% CMA-80 in methylene chloride) 0.3 g (41%) of pure RTI-202 which was further purified by recrystallizing from ether/hexane: ¹H NMR (CDCl₃) δ 1.65 (m, 1H), 1.87 (m, 2 H), 2.24 (m, 2H), 2.34 (s, 3H), 2.41 (m, 1H), 3.28 (m, 2 H), 3.40 (m, 1H), 3.62 (m, 1H), 6.8 (m, 2H), 6.81 (m, 2H), 7.29 (m, 2H), 7.70 (m, 1H), 7.84 (m, 1H); ¹³C NMR (CDCl₃) δ 25.58, 26.07, 35.40, 36.95, 41.56, 53.09, 61.57, 65.47, 120.95, 122.42, 124.11, 125.20, 128.05, 129.03, 131.87, 136.72, 139.91, 151.33, 171.11; IR (CHCl₃) 2940, 2795, 1495, 1445, 1305, 1130, 1105, 1015, 907 CM⁻¹; [α]_(D)−233.89° (c=0.09, OCHC₃).

[0136] The benzothiazole was converted into hydrochloride salt: ¹H NMR (MeOD) δ 2.02 (m, 1H), 2.43 (m, 4H), 2.89 (m, 1H), 2.98 (s, 3H), 3.90 (m, 2H), 4.23 (m, 1H), 4.34 (m, 1H), 7.02 (m, 2H), 7.13 (m, 2H), 7.45 (m, 2H), 7.81 (m, 1H), 8.16 (m, 1H); mp 140-1500C (dec); Anal calcd for C₂₁H₂₂Cl₂N₂S.0.75H₂O C=60.21, H=5.65, N=6.69, Cl=16.93; S=7.65: found C=60.14, H=5.74, N=6.60, Cl=16.89; S=7.71; [α]_(D)−1 72.49° (c 0.28, MeOH).

EXAMPLE 11

[0137] 3β-(4-Chlorophenyl)-tropane-2p-nitrile (RTI-161) To a solution of 0.95 g (3.5 mmol) of 3D-(4-Chlorophenyl)-tropane-2β-carboxamide in 20 ml dry THF was added 0.56 ml (7 mmol) pyridine. To the resulting solution at room temperature was added dropwise with stirring under nitrogen 0.35 ml (4.2 mmol) of trifluoroacetic anhydride. The reaction was stirred at room temperature for 30 minutes, and quenched with 10 ml water. The solvent was removed under vacuo and the residue was taken in 10 ml saturated aqueous K₂CO₃ and extracted thrice with 10 ml CHCl₃. The organic layers were combined and washed with 20 ml brine dried (NaSO₄), filtered, and the solvent removed in vacuo to give 0.26 g crude product. Purification of the crude by flash column chromatography (10% CMA in methylene chloride) gave 0.68 g (77%) of pure nitrile RTI-161 which was recrystallized from methylene chloride and hexane: ¹H is NMR (CDCl₃) δ 1.70 (m, 3H), 2.22 (m, 3H), 2.35 (s, 3H), 2.80 (m, 1H), 3.04 (m, 1H), 3.34 (m, 1H), 3.43 (m, 1H), 7.26 (m, 4H); IR (CHCl₃) 3700, 2950, 2225, 1490, 1470, 1090, 900 cm¹; mp 167-173° C.; Anal calcd for C₁₅H₁₈Cl₂N₂.0.75H₂O; C=57.98, H=6.32 N=9.02, Cl=22.82; found C=58.22, H=6.12, N=8.48, Cl=22.89; [α]_(D)−73.33° (c=0.48, MeOH)

EXAMPLE 12

[0138] 3β-(4-Methylphenyl)-tropane-2β-nitrile Hydrochloride (RTI-158)

[0139] Reaction of 0.26 g (1 mmol) of 3β-(4-Methylphenyl)-tropane-2β-carboxamide as described above for RTI-161 gave after work up and purification 0.16 g (67%) of pure nitrile (RTI-158): ¹H NMR (CDCl₃) δ 1.68 (m, 3H), 2.18 (m, 3H), 2.32 (s, 3H), 2.35 (s, 1H), 2.82 (m, 1H), 3.02 (m, 1H), 3.36 (m, 1H), 3.43 (m, 1H), 7.18 (m, 4H); IR (CHCl₃) 3675, 3000, 2950, 2200, 1600, 1510, 1450, 1350, 1220, 1100 cm⁻¹.

[0140] The crude product was crystallized as the HCl salt: ¹H NMR (MeOH) δ 2.08-2.58 (m, 9H), 2.92 (s, 3H), 3.54 (m, 1H), 3.69 (br s, 1H), 4.12 (br s, 1H), 4.29 (m, 1H), 7.21 (m, 4 H); mp 270° C. (dec.); Anal calcd for C₁₆H₂, CIN₂; C 69.42, H=7.65 N=10.12, Cl=12.81; found C=69.31, H=7.70, N=10.12, Cl=12.81; [α]_(D)−76.4° (c=0.5, MeOH).

EXAMPLE 13

[0141] 3β-(4-Chlorophenyl)-tropane-2β-tetrazole (RTI-163)

[0142] To a solution of 0.13 g 0.5 mmol) of RTI-161 in 5 ml dry THF was added 0.28 ml (5 mmol) azidotrimethylsilane and the mixture was placed in a PTFE-lined autoclave. The solution was heated to 150° C. for 24 hours in an oil bath. The reaction mixture was cooled and transferred using MeOH. The solvent was removed in vacuo to give a brownish residue. Purification of the crude by flash column chromatography (20%-50% CMA in methylene chloride) gave 0.05 g (33.) of pure tetrazole (RTI-163): ¹H NMR (CDCl₃+1 drop MeOD) δ 1.73 (m, 1 H), 2.44-2.02 (m, 4H), 2.6 (m, 1H), 2.68 (s, 3H), 3.33 (m, 1H), 3.65 (m, 1H), 3.73 (m, 1H), 3.97 (m, 1H), 6.68 (d, J=8 Hz, 2H), 7.07 (d, J=8 Hz, 2H); mp 296-300° C.; Anal calcd for C₁₅H₁₈CIN₅.0.75H₂O; C=56.78, H=6.19 N=22.07, Cl=11.17; found C=56.69, H=6.22, N=22.09, Cl=11.15; [α]_(D)−124.94° (c=0.39, MeOH).

EXAMPLE 14

[0143] 3β-(4-Methylphenyl)-tropane-2β-tetrazole Hydrochloride (RTI-157)

[0144] Reaction of 0.12 g (0.5 mmol) of RTI-158 as described above for RTI-163 gave after workup and purification of the crude by flash column chromatography (100% CMA) 0.14 g (88%) of pure tetrazole (RTI-157): ¹H NMR (CDCl₃+1 drop MeOD) δ 1.8 (m, 1H), 2.14 (s, 3H), 2.35 (m, 5H), 2.71 (s, 3H), 3.36 (m, 1H), 3.75 (m, 2H), 4.02 (m, 1H), 6.48 (d, J=8 Hz, 2 H), 6.82 (d, J=8 Hz, 2H).

[0145] The purified product was converted into HCl salt: ¹H NMR (MeOD) δ 2.01 (m, 1H), 2.27 (s, 3H), 2.69 (m, 5H), 2.97 (s, 3H), 3.81 (m, 2H), 4.18 (m, 2H), 5.5 (s, 1H), 6.76 (d, J=8 Hz, 2H), 7.02 (d, J=8 Hz, 2H); mp 212**C. (dec); Anal calcd for C₁₋₆H₂₃Cl₂N₅.0.25H₂O; C=53.26, H=6.56 N=19.41; found C=53.41, H=6.50, N=19.02; [α]_(D)−110.97° (c=0.16, MeOH).

EXAMPLE 15

[0146] 3°-(4-Chlorophenyl)-2β-(3-methylisoxazol-5-yl)tropane Hydrochloride (RTI-165)

[0147] A solution of n-butyl lithium in hexane 5.9 ml (2.5 M. 14.6 mmol) was added to a stirred solution of acetone oxime 0.55 g (7.3 mmol) in dry THF (15 ml) at 0° C. under nitrogen. After 1 hour, a solution of 1.65 g (5.62 mmol) 3p-(4-Chlorophenyl)-2β-(carbomethoxy)tropane in 10 ml dry was added dropwise with stirring at 0° C. The solution was allowed to warm to room temperature over 18 hours. The mixture was poured into a stirred solution of concentrated sulfuric acid (3.2 g) in THF (15 ml) and water (4 ml) and was heated under reflux for 1 hour. The cooled solution was made basic using saturated aqueous K₂CO₃ (10 ml) and extracted thrice with 10 ml methylene chloride. The combined organic layers were dried at (Na₂SO₄), filtered and solvent removed in vacuo to give 1.8 g of crude isoxazole. Purification of the crude residue by flash column chromatography (10° CMA in methylene chloride) gave 0.74 g (46w) of pure isoxazole RTI-165 which was further purified by crystallization from methylene chloride/hexane: !H NMR (CDCl₃) δ 1.71 (m, 3H), 2.10 (m, 3H), 2.18 (s, 3H), 2.24 (s, 3H), 3.20 (m, 2H), 3.32 (m, 2H), 6.18 (s, 1H), 6.9 (d, J=8 Hz, 2H),7.14 (d, J=8, Hz, 2H); IR (CCl₄) 2950, 1590, 1490, 1420, 1350, 1020, 910 cm⁻¹; mp 154-156° C.; Anal calcd for C₁₈H₂₁N₂OCl; C=68.28, H=6.68, N=8.84, Cl=11.19; found C=68.22, H=6.69, N=8.87, Cl=11.19; [α]_(D)−125.58° (c=0.43, MeOH).

[0148] The isoxazole was crystallized as the hydrochloride salt: ¹H NMR (MeOD) δ 2.04 (s, 3H), 2.19 (m, 1H), 2.30 (m, 1H), 2.48 (m, 2H), 2.60 (m, 1H), 2.70 (m, 1H), 2.90 (s, 3H), 3.68 (m, 1H), 3.81 (m, 1H), 4.04 (m, 1H), 4.15 (m, 1H), 5.55 (s, 1H), 7.04 (d, J=8 Hz, 2H), 7.14 (d, J=8 Hz, 2 H); mp>2350C (dec); Anal calcd for C₁₈H₂₂Cl₂N₂O; C=61.19, H=6.28, N=7.93, Cl=20.07; found c=60.98, H=6.38, N=15 7.91, Cl=19.96; [α]_(D)−102.89° (c=0.46, MeOH)

EXAMPLE 16

[0149] 3β-(4-Methylphenyl)-2P-(3-methylisoxazol-5-yl)tropane Hydrochloride (RTI-171)

[0150] Reaction of 1.09 g (4 mmol) of 3β-(4-Methylphenyl)-2β-(carbomethoxy)tropane as described above for RTI-165 gave after workup 1.21 g crude isoxazole. Purification of the crude by flash column chromatography (15% CMA in methylene chloride) gave 0.73 g (62%) pure isoxazole (RTI-171): ¹H NMR (CDCl₃) δ 1.73 (m, 3H), 2.11 (m, 3H), 2.17 (s, 3H), 2.23 (s, 3H), 2.25 (s, 3H), 3.20 (m, 2H), 3.32 (m, 2H), 6.13 (s, 1 H), 6.97 (m, 4H); IR (CCl₄) 2935, 2785, 1590, 1510, 1460, 1421, 1350, 1125,1010, 910 cm⁻¹.

[0151] The isoxazole was crystallized as the hydrochloride salt: ¹H NMR (MeOD) δ 2.01 (s, 3H), 2.24 (s, 3H), 2.32 (m, 2H), 2.42 (m, 4H), 2.81 (s, 3H), 3.61 (m, 1H), 3.78 (m, 1H), 4.03 (m, 1H), 4.15 (m, 1H), 5.45 (s, 1H), 6.96 (m, 4H); mp 277° C.; Anal calcd for Cl₉H₂₅CIN₂O; C=68.55, H=7.57, N 8.42, Cl=10.65; found C=68.65, H=7.62, N=8.42, Cl=10.56; [α]_(D) ^(−107.28°) (c=0.71, MEOH)

EXAMPLE 17

[0152] 3β-(4-Iodophenyl)-2β-(3-methylisoxazol-5-yl)tropane Hydrochloride (RTI-180)

[0153] Reaction of 0.73 g (1.9 mmol) of 3β-(4-Iodophenyl)-2D-(carbomethoxy)tropane as described above for RTI-165 gave after workup 0.77 g of crude isoxazole. Purification of the crude by flash column chromatography (5% CMA80 in methylene chloride) gave 0.37 g (49%) of pure isoxazole RTI-180: ¹H NMR (CDCl₃) δ 1.71 (m, 3H), 2.12 (m, 3H), 2.18 (s, 3H), 2.24 (s, 3H), 3.17 (m, 2H), 3.33 (m, 2H), 6.18 (s, 1H), 6.74 (m, 2 H), 7.49 (m, 2H); IR (CHCl₃) 2940, 1600, 1485, 1450, 1420, 1355 cm⁻¹.

[0154] The isoxazole was crystallized as the hydrochloride salt: ¹H NMR (MeOD) δ 2.11 (s, 3H), 2.50 (m, 6H), 2.89 (s, 3H), 3.70 (m, 1H), 3.90 (m, 1H), 4.14 (m, 1H), 4.22 (m, 1H), 5.66 (s, 1H), 6.96 (m, 2H), 7.56 (m, 2H); mp >235° C. (dec); Anal calcd for C₁₈H₂₂ClIN₂O.25H₂O C=48.12, H 5.05, N=6.24, Cl=15.79; I=56.50; found C=47.84, H=5.05, N=6.19, Cl=15.77; I=56.46; [α]D ⁻94.57° (c=0.39, MeOH)

EXAMPLE 18

[0155] 3β-(4-Chlorophenyl)-2β-(3-phenylisoxazol-5-yl)tropane Hydrochloride (RTI-177)

[0156] Reaction of 1.18 g (4 mmol) of 3β-(4-Chlorophenyl)-2β-(carbomethoxy)tropane as described above for RTI-165 gave after work up 1.46 g of crude isoxazole. Purification of the crude by flash column chromatography [20% (ether/triethylamine 9:1) in hexane] gave 0.75 g (50%) of pure isoxazole RTI-177 which was further purified by crystallizing from ether/petroleum ether: ¹H NMR (CDCl₃) δ 1.74 (m, 3H), 2.22 (m, 3H), 2.27 (s, 3H), 3.24 (m, 2H), 3.36 (m, 2H), 6.80 (s, 1 H), 6.94 (m, 2H), 7.12 (m, 2H), 7.40 (m, 3H), 7.76 (m, 2 H); IR (CHCl₃) 2940, 1600, 1590, 1490, 1450, 1405, 1350 cm⁻¹.

[0157] The isoxazole was crystallized as the hydrochloride salt: ¹H NMR (MeOD) δ 2.35 (m, 6H), 2.84 (s, 3H), 3.73 (m, 1 H;, 4.09 (m, 1H), 4.21 (m, 1H), 6.12 (s, 1H), 7.14 (m, 4H), 7.34 (m, 3H), 7.57 (m, 2H); mp 287° C.; Anal calcd for C₂₃H₂₄Cl₂IN₂O.0.25H₂O C=65.79, H=5.88, N 6.67, Cl=16.89; found C=65.94, H=5.79, N=6.68, Cl=17.00; [α]_(D)−97.5° (c=0.28, MeOH).

EXAMPLE 19

[0158] 3β-(4-Methylphenyl)-2β-(3-phenylisoxazol-5-yl)tropane Hydrochloride (RTI-176)

[0159] Reaction of 1.09 g (4 mmol) of 3β-(4-Methylphenyl)-2β-(carbomethoxy)tropane as described above for RTI-165 gave after work up 1.56 g of crude isoxazole. Purification of the crude by flash column chromatography [25% (ether/triethylamine 9:1) in hexane] gave 1.1 g (77w) of pure isoxazole RTI-176 which was further purified by crystallizing from methylene chloride/hexane: ¹H NMR (CDCl₃) δ 1.76 (m, 3H), 2.23 (m, 3H), 2.24 (s, 3H), 2.27 (s, 3H), 3.23 (m, 2H), 3.36 (m, 2H), 6.74 (s, 1H), 6.93 (m, 4H), 7.41 (m, 3H), 7.76 (m, 2H); IR (CCl₄) 2935, 1590, 1455, 1410, 1215 cm¹

[0160] The isoxazole was crystallized as the hydrochloride salt: ¹H NMR (MeOD) δ 2.08 (m, 1H), 2.15 (s, 3H), 2.45 (m, 5H), 2.84 (s, 3H), 3.68 (m, 1H), 3.88 (m, 1H), 4.07 (m, 1H), 4.22 (m, 1H), 5.97 (s, 1H), 7.0 (m, 4H), 7.33 (m, 3H), 7.54 (m, 2H); mp 270-295° C. (dec); Anal calcd for C₂₄H₂₇CIN₂O; C=72.99, H=6.89, N=7.10, Cl=8.98; found C=72.91, H=6.91, N=7.15, Cl=8.98; [α]_(D)−102.22 (c=0.68, MeOH)

EXAMPLE 20

[0161] 3β-(4-Iodophenyl)-2w-(3-phenylisoxazol-5-yl)tropane Hydrochloride (RTI-181)

[0162] Reaction of 0.73 g (1.9 mmol) of 30-(4-Iodophenyl)-2β-(carbomethoxy)tropane as described above for RTI-181 gave after workup 1.46 g of crude isoxazole. Purification of the crude by flash column chromatography [20% (ether/triethylamine 9:1) in hexane] gave 0.5 g (56%) of pure isoxazole RTI-181 which was further purified by crystallizing from methylene chloride/hexane: ¹H NMR (CDCl₃) δ 1.72 (m, 3H), 2.15 (m, 2H), 2.28 (s, 3H), 3.22 (m, 2H), 3.35 (m, 2H), 6.74 (m, 2H), 6.79 (s, 1H), 7.44 (m, 5H), 7.75 (m, 2H); IR (CHCl₃) 2940, 1580, 1480, 1475, 1450, 1400, 1355, 1005 cm⁻¹

[0163] The isoxazole was crystallized as the hydrochloride salt: 1 H NMR (MeOD) δ 2.54 (m, 6H), 2.92 (s, 3H), 3.79 (m, 1H), 4.05 (m, 1H), 4.19 (m, 1H), 4.33 (m, 1H), 6.18 (s, 1H), 7.02 (m, 2H), 7.43 (m, 3H), 7.63 (m, 4H); mp >2677C (dec); Anal calcd for C₂₃H₂₄ClIN₂O.0.5H₂O C=53.55, H=4.89, N=5.43, Cl=13.75; I=49.21: found C=53.75, H=4.87, N=5.41, Cl=13.68; I=48.95; [α]_(D)−91.11° (c=0.43, MeOH)

EXAMPLE 21

[0164] Biochemistry of 3α-(Substituted phenyl)-2β-(heterocyclic)tropanes

[0165] Inhibition of radioligand binding data at the dopamine, serotonin, and norepinephrine transporters are listed in Tables II, III and IV. TABLE II 3β-(Substituted phenyl)-2β-(heterocyclic)tropanes A

IC₅₀ (nM) Code DA NE 5-HT NE/DA 5-HT/D Name Het X [³H]-WIN 35,428 [³H]-nisoxetine [³H]-paroxatine Ratio Ratio RTI-163 RTI-157

Cl CH₃   911 ± 6.1 1557 ± 196 17,386 ± 2050 32,478 ± 2078   5456 ± 64 43,574 ± 5420 19 21 6 28 RTI-165 RTI-171 RTI-180

Cl CH₃I  0.59 ± 0.04  0.93 ± 0.09  0.73 ± 0.04   181 ± 12   254 ± 31  67.9 ± 5.25   572 ± 58   3818 ± 346  36.4 ± 5.0 307 273 93 970 4105 498 RTI-177 RTI-176 RTI-181

Cl CH₃I  1.28 ± 0.18  1.58 ± 0.02  2.57 ± 0.14   504 ± 29   398 ± 18   868 ± 95   2418 ± 136   5110 ± 187   100 ± 9.0 393 251 337 1889 3234 39 RTI-189 RTI-178

Cl CH₃  19.7 ± 1.98  35.4 ± 1.74   496 ± 42   677 ± 68   1116 ± 107   1699 ± 167 25 19 57 48 RTI-188 RTI-195

Cl CH₃  12.6 ± 1.03  47.5 ± 4.76   929 ± 88   1310 ± 37   3304 ± 196 23,310 ± 822 73 28 262 491 RTI-194

CH₃  4.45 ± 0.12   253 ± 19   4885 ± 155 57 1098 RTI-200 RTI-199

Cl CH₃  15.3 ± 2.43  35.9 ± 3.4   4142 ± 466 24,321 ± 3822 18,417 ± 1509 51,460 ± 4513 271 677 1203 1434 RTI-202

Cl  1.37 ± 0.14   403 ± 30   1119 ± 120 294 817 RTI-219

Cl   571 ± 0.36   8563 ± 824 10,342 ± 76 1500 1811

[0166] TABLE III Comparison of Transporter Binding Potencies

IC₅₀ (Nm) RTI 5-HT DA NE No. R₁ R₂ [³H] Paroxetine [³H] WIN 35,428 [³H] Nisoxetine 279 CH₃ CH₃ 1.06 ± 0.39 5.98 ± 0.48 74.3 ± 3.8 353 C₂H₅ CH₃ 0.69 ± 0.07  331 ± 17  148 ± 9.2 Paroxetine* 0.28 ± 0.02  623 ± 25 313

[0167] TABLE IV 3β-(Substituted phenyl)-2β-(substituted)tropanes

IC₅₀ (nM) Code DA NE 5-HT Name R X [³H]-WIN 35,428 [³H]-nisoxetine [³H]-paroxetine RTI-93 CH₂OH Cl  1.53 ± 0.15  43.8 ± 6.4   204 ± 16 RTI-99 CH₂OH Br  1.49 ± 0.06   51 ± 45 RTI-100 CH₂OH F   47 ± 4.6  4741 ± 335 RTI-101 CH₂OH I  2.2 ± 0.19   26 ± 32 RTI-102 CO₂H I   474 ± 57 43,400 ± 5600  1928 ± 120 RTI-103 CO₂H Br   278 ± 43 17,400 ± 1400  3070 ± 208 RTI-104 CO₂H F  2744 ± 141 >100,000 >100.00 RTI-105 CH₂OAc Cl  1.60 ± 0.06   127 ± 5.9   143 ± 25 RTI-108 CH₂Cl Cl  2.64 ± 0.31   129 ± 15   98 ± 8.7 RTI-123 CH₂OCOC₆H₅ Cl  1.78 ± 0.09   383 ± 30   353 ± 058 RTI-131 CH₂NH₂ CH₃  10.5 ± 1.7   120 ± 20   855 ± 52 RTI-132 CH₂N(CH₃)₂ CH₃  3.48 ± 0.11   137 ± 11   208 ± 18 RTI-139 CH₃ Cl  1.87 ± 0.13    57 ± 2.6   85 ± 93 RTI-145 CH₂OCO₂CH₃ Cl  9.6 ± 0.42   1478 ± 96  2930 ± 181 RTI-158 CN CH₃   57 ± 7.3   1824 ± 138  5095 ± 315 RTI-161 CN Cl  13.1 ± 0.78   2516 ± 253  1887 ± 134 RTI-164 CH₂NHCH₃ CH₃  13.6 ± 2.03   280 ± 19  2246 ± 94 RTI-230 —C(CH₃)═CH₂ Cl  1.28 ± 0.17   141 ± 16   57 ± 50 RTI-239 CH(CH₃)₂ CH₃  0.61 ± 0.07  35.6 ± 2.57   114 ± 369 RTI-240 CH(CH₃)₂ Cl   138 ± 0.03  84.5 ± 3.09  38.4 ± 2.31 RTI-241 CH₂CO₂CH₃ CH₃  1.02 ± 0.06   124 ± 3.56   618 ± 28

[0168] This invention has been described in both generic terms, and by reference to specific description. No specific description or example is considered binding, unless so identified. Alternate forms and methods will occur to those of ordinary skill in the art, without the exercise of inventive faculty, and remain within the scope of this invention, save as limited by the claims set forth below. 

What is claimed is:
 1. A compound of the formula:

wherein R₁ is H or CO₂CH₃.
 2. A compound of the formula:

wherein R₁=CH₃, Y=CO₂CH₃, M=C≡C X=H, Z=H.
 3. A compound of the formula:

wherein X=CH₃ or H and Y=CH₃ or H.
 4. The compound of claim 3, wherein X=CH₃ and Y=H.
 5. A compound of the formula:

wherein R₁, R₂=H or CH₃ and X=CH₃.
 6. A compound of the formula:

wherein R₁=CH₃, C₆H₅, 4-CH₃OC₆H₄, 4-ClC₆H₄, 4-BrC₆H₄, or (CH₃)₂CH and X=H, Cl or CH₃.
 7. The compound of claim 6, wherein R₁ is 4-BrC₆H₄ and X is Cl.
 8. A compound of the formula:

wherein R=CH₃, CH₂CO₂C₂H₅ or H and X=t-CH₃CH═CH, CH₃C≡C, HC≡C, H₂C═C, Cl, or 2-naphthyl.
 9. The compound of claim 8, wherein X is 2-naphthyl and R is Cl₃.
 10. The compound of claim 8, wherein X is Cl and R is CH₄CO₂C₂H₅.
 11. The compound of claim 8, wherein X is H₂C═C and R is H.
 12. The compound of claim 8, wherein X is t-CH₃CH═CH and R is CH₃.
 13. A compound of the formula:

wherein X=CH₃ or Cl and


14. The compound of claim 13, wherein R is CH(CH₃)₂ and X is CH₃.
 15. The compound of claim 13, wherein R is CH₂OCOC₆H₅ and X is Cl.
 16. The compound of claim 13, wherein


17. The compound of claim 13, wherein


18. The compound of claim 13, wherein


19. A compound of tile formula:

wherein R_(b) is C₂H₅, CH(CH₃)₂, or C₆H₅, X is CH₃ or Cl and Z is H. 